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Merck
  • Active elimination of intestinal cells drives oncogenic growth in organoids.

Active elimination of intestinal cells drives oncogenic growth in organoids.

Cell reports (2021-07-08)
Ana Krotenberg Garcia, Arianna Fumagalli, Huy Quang Le, Rene Jackstadt, Tamsin Rosemary Margaret Lannagan, Owen James Sansom, Jacco van Rheenen, Saskia Jacoba Elisabeth Suijkerbuijk
摘要

Competitive cell interactions play a crucial role in quality control during development and homeostasis. Here, we show that cancer cells use such interactions to actively eliminate wild-type intestine cells in enteroid monolayers and organoids. This apoptosis-dependent process boosts proliferation of intestinal cancer cells. The remaining wild-type population activates markers of primitive epithelia and transits to a fetal-like state. Prevention of this cell-state transition avoids elimination of wild-type cells and, importantly, limits the proliferation of cancer cells. Jun N-terminal kinase (JNK) signaling is activated in competing cells and is required for cell-state change and elimination of wild-type cells. Thus, cell competition drives growth of cancer cells by active out-competition of wild-type cells through forced cell death and cell-state change in a JNK-dependent manner.

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Sigma-Aldrich
多西环素 单盐酸半乙醇半水合物
Sigma-Aldrich
N-乙酰基-L-半胱氨酸, BioReagent, suitable for cell culture
Sigma-Aldrich
抗磷酸组蛋白H3(Ser10)抗体,有丝分裂标记, Upstate®, from rabbit
Sigma-Aldrich
JNK-IN-8, ≥96% (HPLC)